ルイス酸性,非無害なアンチモニーリガンドによるプラチナ複合体の触媒活性を解明
1Department of Chemistry, Texas A&M University , College Station, Texas 77843, United States.
Journal of the American Chemical Society
|May 10, 2017
まとめ
研究者らはルイス酸性アンチモンのリガンドを含む自己活性化プラチナ触媒を開発した. この新しい複合体は,室温でエニンの循環と水酸化のようなアルキンの反応を効率的に触媒化します.
科学分野:
- 有機金属化学
- カタリシス
- メイングループ 化学
背景:
- 効率的な化学合成のために,自己活性化電化触媒の開発が不可欠です.
- 移行金属の中心付近のルイス酸分子は触媒活性を増強する.
研究 の 目的:
- 隣接するルイス酸性アンチモンの中心を持つ新しいプラチナ複合体を合成し,特徴づけること.
- 有機変換におけるこの複合体の触媒的可能性を調査する.
主な方法:
- シルバートリフラートによるプラチナ前駆体処理によるプラチナ-アンチモニー複合体の合成.
- 結果的な複合体の特徴
- アルキン反応の触媒としての複合体の評価,アルキンサイクリングと分子内ヒドロアリレーションを含む.
主要な成果:
- 安定したプラチナ複合体 ((o- ((Ph2P) C6H4) 2SbOTf2) PtCl (2) が合成された.
- 複合体2は分子内ハライド抽出を行い,プラチナセンターを活性化します.
- 複合体は,外部アクティベータなしで室温でエニンサイクルと分子内水酸化反応を効果的に触媒化しました.
結論:
- アンチモンの配合非無罪性は,自己活性化電化触媒に利用できる.
- この研究は,効率的で自己活性化可能な移行金属触媒の設計のための新しい戦略を提示しています.
さらに関連する動画
関連する概念動画
Metal-Ligand Bonds
24.9K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
24.9K
Radical Substitution: Hydrogenolysis of Alkyl Halides with Tributyltin Hydride
2.3K
Radical substitution reactions can be used to remove functional groups from molecules. The hydrogenolysis of alkyl halides is one such reaction, where the weak Sn–H bond in tributyltin hydride reacts with alkyl halides to form alkanes. Here, the reagent Bu3SnH yields tributyltin halide as a byproduct.
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
The bonds formed in this reaction are stronger than the bonds broken, making it energetically favorable. The reaction follows a radical chain mechanism similar to radical halogenation reactions,...
2.3K
Valence Bond Theory
11.4K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
11.4K
Formation of Complex Ions
26.5K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
26.5K
Complexation Equilibria: Factors Influencing Stability of Complexes
892
In complexation reactions, metal cations are the electron pair acceptors, and the ligands are the electron pair donors. The stability of the metal complexes depends primarily on the complexing ability of the central metal ion and the nature of the ligands. Generally, the complexing ability of the metal ion depends on the size and charge of the ion. As the metal ion size increases, the stability of the metal complexes decreases, provided that the valency of the metal ion and the ligands remain...
892
Electrophilic Aromatic Substitution: Sulfonation of Benzene
8.7K
Sulfonation of benzene is a reaction wherein benzene is treated with fuming sulfuric acid at room temperature to produce benzenesulfonic acid. Fuming sulfuric acid is a mixture of sulfur trioxide and concentrated sulfuric acid.
8.7K


